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Stereospecific Construction of Contiguous Quaternary All-Carbon Centers by Oxidative Ring Contraction
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文摘
Oxidative ring contraction of cyclic α-formyl ketones was facilitated by the action of H2O2 under operationally simple and environmentally benign reaction conditions. The process was highly regioselective and enables stereospecific construction of contiguous quaternary all-carbon centers from stereodefined all-substituted all-cyclic ketones. The asymmetric syntheses of (+)-cuparene and (+)-tochuinyl acetate were also successively achieved by taking advantage of this novel protocol.

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